Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069059Generated: October 30, 2026

Water → tert-Butyl 4-(1-hydroxypropan-2-yl)pyridin-2-ylcarbamate

https://huagongshe.com/reaction/2069059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantEthyl 2-(2-(tert-butoxycarbonylamino)pyridin-4-yl)propanoateHCID 58532575—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(1-hydroxypropan-2-yl)pyridin-2-ylcarbamateHCID 5853258153.5%

Reaction Steps

A solution of DIBAL (1M in DCM, 13.8 mL, 13.8 mmol) was added dropwise over 10 min to a stirred solution of the ester (52) (1.35 g, 4.59 mmol) in THF (25 mL) under nitrogen at −78° C. The reaction mixture was warmed to RT and then re-cooled to −78° C. and a second aliquot of DIBAL (1M in DCM, 4.5 mL, 4.5 mmol) was added. The reaction mixture was allowed to warm to RT, then cooled to 0° C. and water (5 mL) and then MgSO4 were added. The mixture was diluted with DCM and filtered to remove the solids. The filter cake was washed with EtOAc, MeOH and DCM and the combined filtrate and washings were evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 40 g, 25-50% EtOAc in isohexane, gradient elution) to afford the title compound (53) (0.62 g, 50%): m/z 253 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-7249bd5261d441cb895714ab6704fdff
Source noteuspto-grants-2012_10